Phenylthiocarbamoylguanidine hydrochloride

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Identification

Molecular formula
C9H14ClN3S
CAS Number
27887-98-1
IUPAC Name
[N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl]ammonium;chloride
Molecular Weight
243.74g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2905g/cm3
Interesting facts

Interesting Facts about N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl Ammonium Chloride

The compound N-phenyl-N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride is an intriguing member of the class of compounds known as thioureas. This compound, characterized by its unique functional groups, possesses various applications in the fields of chemistry and medicinal science. Here are some interesting insights:

  • Dual Functionality: This compound features both an ammonium group and a sulfhydryl (thiol) moiety, which could allow it to participate in a variety of chemical reactions, making it a versatile building block in medicinal chemistry.
  • Biological Relevance: Compounds like this one are often explored for their potential bioactivity. Thiol groups are known to participate in redox reactions, which are critical in biological systems.
  • Potential Applications: Researchers are examining the utility of thiourea derivatives in drug development and as catalysts in organic synthesis, due to their ability to stabilize reactive intermediates and facilitate transformations.
  • Analytical Importance: Its unique structural features make it a candidate for exploration in analytical chemistry, particularly in the development of new methods for detection and quantification of biomolecules.

Furthermore, the presence of both electron-donating and electron-withdrawing elements in the structure can profoundly affect the compound's reactivity and stability. As one researcher eloquently noted, “The beauty of chemistry lies in the vastness of possibilities that each molecule can present.” This compound exemplifies that beauty, opening up numerous pathways for exploration in both academic research and practical applications.


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